Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47650 | A09 | 51824123 | C | T | upstream_gene_variant | MODIFIER | c.-3991C>T| |
S68 |
2 | BAA09g47650 | A09 | 51824732 | G | A | upstream_gene_variant | MODIFIER | c.-3382G>A| |
S278 |
3 | BAA09g47650 | A09 | 51824953 | C | T | upstream_gene_variant | MODIFIER | c.-3161C>T| |
S259 |
4 | BAA09g47650 | A09 | 51825148 | G | A | upstream_gene_variant | MODIFIER | c.-2966G>A| |
S81 S85 |
5 | BAA09g47650 | A09 | 51825152 | C | T | upstream_gene_variant | MODIFIER | c.-2962C>T| |
S205 |
6 | BAA09g47650 | A09 | 51825252 | G | A | upstream_gene_variant | MODIFIER | c.-2862G>A| |
S255 |
7 | BAA09g47650 | A09 | 51828189 | G | A | missense_variant | MODERATE | c.76G>A|p.Glu26Lys |
S247 |
8 | BAA09g47650 | A09 | 51828375 | G | A | missense_variant | MODERATE | c.262G>A|p.Val88Ile |
S308 |
9 | BAA09g47650 | A09 | 51828670 | G | A | missense_variant | MODERATE | c.557G>A|p.Gly186Glu |
S116 |
10 | BAA09g47650 | A09 | 51831259 | G | A | downstream_gene_variant | MODIFIER | c.*2507G>A| |
S135 |
11 | BAA09g47650 | A09 | 51831624 | C | T | downstream_gene_variant | MODIFIER | c.*2872C>T| |
S224 |
12 | BAA09g47650 | A09 | 51833459 | G | A | downstream_gene_variant | MODIFIER | c.*4707G>A| |
S166 |